BEGIN:VCALENDAR VERSION:2.0 PRODID:-//ChamberMaster//Event Calendar 2.0//EN METHOD:PUBLISH X-PUBLISHED-TTL:P1H REFRESH-INTERVAL:P1H CALSCALE:GREGORIAN BEGIN:VTIMEZONE TZID:America/New_York BEGIN:DAYLIGHT RRULE:FREQ=YEARLY;BYMONTH=3;BYDAY=2SU DTSTART:20070101T000000 TZOFFSETFROM:-0500 TZOFFSETTO:-0400 TZNAME:Eastern Daylight Time END:DAYLIGHT BEGIN:STANDARD RRULE:FREQ=YEARLY;BYMONTH=11;BYDAY=1SU DTSTART:20070101T000000 TZOFFSETFROM:-0400 TZOFFSETTO:-0500 TZNAME:Eastern Standard Time END:STANDARD END:VTIMEZONE BEGIN:VEVENT DTSTART;TZID=America/New_York:20210622T090000 DTEND;TZID=America/New_York:20210624T130000 X-MICROSOFT-CDO-ALLDAYEVENT:FALSE SUMMARY:Risk Management True Quality Summit Series DESCRIPTION:WHAT TO EXPECT AT THE RISK MANAGEMENT TRUE QUALITY SUMMIT SERIES BY Greenlight GuruMedical device risk management is not optional it is a regulatory requirement worldwide. But with today's medical device regulatory environment changing faster than ever\, and the confusion that can come with Risk Management\, it doesn't mean it's easy. The Risk Management True Quality Summit Series will help quality\, regulatory and product development professionals and executives understand and implement risk management concepts that can help meet FDA\, ISO 14971\, ISO 13485:2016\, and the MDR 2017/745 requirements for risk management. We'll dive into the standards and outline deliverables at each stage of the risk management process\, explore practical solutions for applying the standards within your organization\, and ultimately give you tools to ensure risk management lives throughout your entire product life cycle. Learn more X-ALT-DESC;FMTTYPE=text/html:
WHAT TO EXPECT AT THE RISK MANAGEMENT TRUE QUALITY SUMMIT SERIES BY Greenlight Guru
Medical device risk management is not optional &ndash\; it is a regulatory requirement worldwide. But with today'\;s medical device regulatory environment changing faster than ever\, and the confusion that can come with Risk Management\, it doesn&rsquo\;t mean it&rsquo\;s easy. \;
The Risk Management True Quality Summit Series will help quality\, regulatory and product development professionals and executives understand and implement risk management concepts that can help meet FDA\, ISO 14971\, ISO 13485:2016\, and the MDR 2017/745 requirements for risk management. \;
We&rsquo\;ll dive into the standards and outline deliverables at each stage of the risk management process\, explore practical solutions for applying the standards within your organization\, and ultimately give you tools to ensure risk management lives throughout your entire product life cycle. \;
LOCATION: UID:e.1244.356759 SEQUENCE:3 DTSTAMP:20240328T155126Z URL:https://business.massmedic.com/events/Details/risk-management-true-quality-summit-series-349856?sourceTypeId=Hub END:VEVENT END:VCALENDAR